Phytogenesis of halomethanes: A product ofselection or a metabolic accident?

Phytoplankton (microalgae), seaweeds(macroalgae), higher plants and fungi producehalomethanes. Algae and fungi produce bothmethyl halides and polyhalomethanes, whereasplants are known to produce only methylhalides. Why these organisms producehalomethanes is a question frequently asked bychemists and biologists. This question impliesthat halomethanes have a function and have aselective value to the producing organism.Except for some fungi, the evolutionaryadvantage of producing halomethanes may notpresently exist. Polyhalomethanes areby-products of halogenation of certain organiccompounds by haloperoxidases in marine algaeand perhaps some fungi, and they may beindirectly produced in aquatic environments byalgal release of oxidized halogen species. Amain function of this enzyme is to rid the cellof harmful oxidants such as hydrogen peroxide.Monohalomethanes (methyl halides) are productsof methyltransferase activity. It has beenproposed that methyl halide production mayprovide a mechanism to regulate chloride levelsin halotolerant plants. The examination of halidecellular concentrations, halomethane productionrates, and enzyme characteristics raisesquestions about this possible function. Inalgae, plants and some fungi, methyl halidesmay be a result of the insertion of ubiquitoushalides into the active site of numerousmethyltransferases. Therefore, halomethanes maybe by-products or `accidents' of metabolism.     

The carbohydrate units of asialo-ovomucoid: structural features

The structural features of a heterogeneous glycopeptide fraction from asialo-ovomucoid have been investigated by methylation analysis of the fraction and of products obtained at each stage of its sequential degradation with exo-glycosidases. All glycopeptides in the fraction had a common core-structure beta-D-GlcpNAc-(1 leads to 4)-[beta-D-GlcpNAc-(1 leads to 2)]-alpha-D-Manp-(1 leads to 3)-[beta-D-GlcpNAc-(1 leads to 4)]-[beta-D-GlcpNAc-(1 leads to 2)-alpha-D-Manp-(1 leads to 6)]-beta-D-Manp-(1 leads to 4)-beta-D-GlcpNAc-(1 leads to 4)-beta-D-GlcpNAc leads to Asn. Heterogeneity in the fraction arose from variation in the amount of terminal galactose attached via a hexosaminyl residue to the alpha-D-Manp-(1 leads to 3) residue, and from limited variation in the number of terminal hexosaminyl groups attached to the alpha-D-Manp-(1 leads to 6) residue. One glycopeptide in the fraction contained the unusual feature of two different, triply-substituted mannosyl residues. Other structural features of the glycopeptide are discussed.     

The units of currency for plant water status

Abstract. The appropriate measure for plant water status is of fundamental importance in plant water relations. One possible approach is to consider a hypothetical sensor for water status at the cell level. It is argued that such a sensor must respond to an intrinsic variable describing the quantity of water present in the cell. Uncertainty about the variable being sensed has affected our interpretion of plant responses to drought. In general, a more rigorous analysis of the effects of tissue hydraulic parameters and further understanding of the pertinent variable for water status are needed to assess such questions. For example, the significance of changes in the elasticity of cell walls in response to drought depends on the measure for water status. A simple model for water transport suggests that a decrease in the elastic modulus may act to maintain turgor for succulent plant species, but it is not clear how increases in the elastic modulus enhance water uptake for non-succulent species.     

The functional units of a peptostreptococcal protein L

Protein L is a cell-surface protein from Peptostreptococcus which interacts with immunoglobulin kappa light chains. A gene from Peptostreptococcus strain 3316 coding for protein L and fragments thereof were expressed in Escherichia coli. The peptides were examined for binding to immunoglobulin and serum albumin. The four C units were shown to be responsible for binding to immunoglobulin and the four D units for binding to albumin. This protein L molecule therefore binds to albumin at a site separate from that involved in binding to immunoglobulin. The albumin-binding units have high amino acid sequence identity with the albumin-binding units of streptococcal cell-surface proteins. The gene contains three sites available for internal initiation of translation resulting in three active proteins. The protein L molecule presented in this report was compared with a previously reported protein from Peptostreptococcus strain 312. The two proteins differ in several respects, including size and the number and types of repeat units.     

The units of selection and measures of fitness

This paper presents a unified account of the properties of the measures, Malthusian parameter and entropy in predicting evolutionary change in populations of macromolecules, cells and individuals. The Malthusian parameter describes the intrinsic rate of increase of the population. The entropy describes the intrinsic variability in populations: it characterizes the variability in mutation and replication rates in populations of macromolecules; the rate of decay of synchrony in populations of cells; and the degree of iteroparity in populations of individuals. The Malthusian parameter determines ultimate population numbers: under constant environmental conditions, it is the rate of increase when equilibrium conditions are attained. Entropy determines population stability: the gain in the Malthusian parameter due to small fluctuations in the life-cycle variables is determined by entropy. These properties, which are valid for populations of macromolecules, cells and individuals, show that the Malthusian parameter and entropy act as complimentary fitness indices in understanding evolutionary change in populations.     

The units of DNA replication in the mammalian chromosomes: Evidence for a large size of replication units

The replication of chromosomal DNA in human and Chinese hamster cell populations has been studied by means of the DNA fiber autoradiography. It was found that the rate of DNA replication for one fork in human cells varies from 0.2 to 0.9 m/min, the average being 0.6 m/min. In the Chinese hamster cells the rate of DNA replication is greater, varying from 0.3 to 1.2 m/min, the average being 0.8 m/min. There are no clusters containing a great number of replication units in human and Chinese hamster cells. Sequences consisting of two or three replicons which belong to single DNA molecule have been observed, but their frequency was relatively low. The distances between the initiation points in such sequences of replicons vary from 40 to 280 m, the average value being 130 m. This value represents the minimum size of the replication units which have completed the DNA synthesis within 3 h of the S-period. The DNA synthesis in most replication units fails to be accomplished within the three hours of labelling. The process can be completed only in the fragments of DNA molecules of 40 to 200 m (the average value being 100 m) in human cells, whereas in the Chinese hamster cells the fragments of 40 to 250 m (the average being about 140 m) are completely replicated. Provided that the replication is bidirectional the complete replicons are supposed to contain two such fragments. Consequently, the greater part of replication units in mammalian cells covers the pieces of a few hundred microns in DNA molecules. The relation between replication process at the DNA molecules level and that at the metaphase chromosome level is discussed.